Mechanistic and therapeutic links between rheumatoid arthritis and diabetes mellitus.
Jing LiYazhuo ChenQingyun LiuZhufang TianYan ZhangPublished in: Clinical and experimental medicine (2022)
Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by persistent synovial inflammation and irreversible cartilage and bone damage. Despite its predominant osteoarticular and periarticular manifestations, RA is also a systematic disease associated with organ-specific extra-articular manifestation. Increasing evidence indicates that RA patients are susceptible to diabetes mellitus (DM), and RA aggravates metabolic disordered in DM, indicating the close association between RA and DM. Many factors involved in RA stimulate insulin resistance and DM development. These factors include proinflammatory cytokines (such as TNF-α, IL-6, IL-1β), RA autoantibodies (such as rheumatoid factor, cyclic citrullinated peptide antibodies), excess RA related adipokines (such as leptin, resistin, ANGPTL4), C-creative protein, and other protein (such as TXNDC5, NLRP3, RBP4). Furthermore, commonly used RA drugs, such as conventional synthetic disease-modifying antirheumatic drugs (csDMARDs), biological disease-modifying antirheumatic drugs (bDMARDs), and glucocorticoids, provide potential benefits in improving insulin resistance and inhibiting DM development. This review discusses the mechanistic and therapeutic links between RA and DM, aiming to provide valuable information for the prevention and treatment of DM in RA patients.
Keyphrases
- rheumatoid arthritis
- disease activity
- ankylosing spondylitis
- insulin resistance
- rheumatoid arthritis patients
- interstitial lung disease
- glycemic control
- end stage renal disease
- systemic lupus erythematosus
- newly diagnosed
- chronic kidney disease
- ejection fraction
- metabolic syndrome
- type diabetes
- prognostic factors
- oxidative stress
- multiple sclerosis
- signaling pathway
- climate change
- risk assessment
- patient reported
- postmenopausal women
- health information
- social media
- drug induced
- combination therapy